Compounds

Details Compounds Compounds

2001-01-04

2001-09-04

Barts, Samuel (Department: 1621)

Organic compounds -- part of the class 532-570 series

Organic compounds

Amino nitrogen containing

C564S082000, C564S083000, C560S045000, C560S056000, C562S467000, C548S156000

Reexamination Certificate

active

06284924

ABSTRACT:

TECHNICAL FIELD
The present invention relates to a novel compound useful as a structural component of polymers such as polyesters and polyamides.
BACKGROUND ART
Liquid crystal polyesters are consisted of rigid molecules which do not entangle even under the melting condition and form crystalline polydomains. The liquid crystal polyesters have low shear properties to realize a remarkably high orientation of molecular chains towards the flow. Generally, said liquid crystal polyesters are called as melted type liquid crystals or thermotropic liquid crystals. Because of their specific behaviors, said polyesters exhibit excellent melt flow properties and provide thin-wall molded articies of 0.2 through 0.5 mm in thickness Although said articles exhibit high strength and high rigidity, they have some disadvantages, including extremely large anisotropy and insufficient weld strength.
DISCLOSURE OF INVENTION
The present invention provides a novel compound which may be useful as a structural component of polyesters, polyamides or the like.
Accordingly, the present invention provides a novel compound obtainable from 2-hydroxynaphthalene-3,6-dicarboxylic acid as a starting material. This compound is important as a multifunctional monomer, which is used to prepare polyesters or polyamides with mesh or ladder structure. For example, a polyester or polyamide prepared with the compound as a structural component is expected to have significantly improved weld strength and anisotropy.
The present invention provides a compound represented by the general formula (1)
wherein Y
1
, Y
2
, Y
3
, and Y
4
may be the same or different and represent carboxy group, an esterified carboxy group or a group of —(CONH)n—X (wherein X is an optionally branched and optionally substituted hydrocarbon group which may have unsaturated bonds, an optionally substituted aromatic group or a heterocyclic group having conjugated double bonds);
n is an integer of 1 or 2;
Q and Q′ each represent an optionally branched alkyl or alkoxy group of 1-6 carbon atoms, a halogen atom, nitro group or nitroso group;
m and m′ each represent an integer of 0-3; and
A represents an optionally substituted and optionally branched bivalent hydrocarbon group of 1-20 carbon atoms which may have unsaturated bonds, wherein said hydrocarbon group may have a moiety of an optionally substituted aromatic group or a heterocyclic group having conjugated double bonds;
or a salt thereof.
In the above formula, preferable esterified carboxylic groups of Y
1
, Y
2
, Y
3
and Y
4
include an alkoxycarbonyl group of 1-6 carbon atoms, especially, methoxy carbonyl and ethoxy carbonyl groups, phenoxy carbonyl group and phenacyl carbonyl group, wherein the aromatic moiety included in the group may have a substituent. X may include an optionally branched and optionally substituted hydrocarbon group which may have unsaturated bonds. Preferably, X may be an alkyl group of 1-20 carbon atoms, an optionally substituted aromatic group such as phenyl, naphthyl and anthraquinonyl, or an optionally substituted heterocyclic group having conjugated double bonds, such as benzimidazolonyl, carbazolyl, pyridyl, thiazolyl, benzothiazolyl, imidazolyl, indolyl, thiofuryl phenothiazinyl, acridinyl, or quinolinyl group.
Examples of substituents on those groups as above may include a halogen atom, nitro, a lower alkyl, a lower alkoxy (e.g. methoxy), cyano, phenoxy, an amidated carboxy (e.g. phenylaminocarbonyl), an esterified carboxy (e.g. methoxycarbonyl, phenoxycarbonyl), and a dialkylamino sulfonyl (e.g. diethylamino sulfonyl) groups.
When the substituent contains an aromatic ring, the compound may further have one or more substituents such as a halogen atom, a lower alkyl, a lower alkoxy, phenyl, and nitrile groups on said aromatic ring. In the present application “lower” represents a group having 1-6 carbon atoms.
In the present invention, each of the two naphthalene nuclei may have substituents of Q or Q′ respectively. Each of Q and Q′ may represent an optionally branched alkyl or alkoxy group of 1-6, preferably 1-4 carbon atoms, a halogen atom, nitro group and nitroso group. Each of m and m′, which represents the number of the substituent, is usually 0 and may be up to 3.
In the above formula, examples of the “optionally substituted and optionally branched bivalent hydrocarbon group of 1-20 carbon atoms which may have unsaturated bonds” of A include an alkylene group (preferably a straight chain alkylene group of 1-12 carbon atoms), an alkenylene group (preferably a straight chain alkenylene group of 1-12 carbon atoms such as 2-butenylene), and an alkylene group which may have a substituent such as oxo group (preferably carbonyl, oxalyl, methylenecarbonyl and dioxo octamethylene group). Said hydrocarbon group may have a moiety of an optionally substituted aromatic group or a heterocyclic group having conjugated double bonds. Examples of the alkylene groups having therein a moiety of an aromatic group or a heterocyclic ring having conjugated double bonds include the group represented by the formulae (2) and (3). Further, a group having one or two oxo groups at the end of A, such as those represented by the formula (4), is also preferably used.
Examples of salts of the compound of the general formula (1), such as a compound wherein any one of Y
1
, Y
2
, Y
3
and Y
4
is carboxy group, include sodium salt and potassium salt thereof.
In one embodiment, the compound of formula (1) may be prepared according to the following scheme:
wherein Y
1
, Y
2
, Y
3
, Y
4
, Q, Q′, m, m′ and A are the same as above.
This reaction may usually be carried out in a conventional medium such as dimethyl formamide, under the presence of a base such as potassium carbonate. In addition, the obtained salt may be hydrolyzed, if desired, to give a carboxylic acid. In the above reaction formula, the dibromo compound (6) is used as one embodiment and other dihalogenated compound such as a dichloro compound may also be used in stead of the dibromo compound.
In another embodiment, a bisether compound of the formula (1) wherein Y
1
, Y
2
, Y
3
and Y
4
are different each other or wherein the molecule is asymmetric, may be prepared, for example, according to the following scheme:
wherein, Y
1
, Y
2
, Y
3
, Y
4
, Q, Q′, m, m′ and A are the same as above.
According to this embodiment, the mono ether compound (10) may be obtained by reacting the naphthol with a base (such as potassium carbonate), in the presence of a bromo-chloro compound (9), in stead of the dibromo compound (6) used in the above method, in a solvent (such as dimethyl formamide). Then the compound (11) having substituents to provide an asymmetric compound may be reacted to give the asymmetric bisether compound (12). The asymmetric compound of the present invention may be hydrolyzed to give a carboxylic acid in the same manner as of the above-described symmetric compound.
In a embodiment wherein A has one or two oxo groups on the carbon atoms at its one or both ends, the compound of the formula (1) may be obtained in the same manner as above by using a dibrominated- or dichlorinated-A compound. Alternatively, when A is a carboxylic acid or an ester thereof, the compound of formula (1) may be prepared by dehydration condensation reaction between A and 2-hydroxynaphthalene-3,6-dicarboxylic acid (8), or by ester exchanging reaction or some other well-known method.
Although an already esterified or amidated naphthol compound was then bisetherized to provide the desired compound in the above described method, the compound may be prepared by bisetherize the naphthol firstly and then esterify or amidate it. The order of the reaction is not limited.
The compound of the present invention is especially useful as a structural component polymers such as polyesters and polyamides.


REFERENCES:
patent: 60-215648 (1985-10-01), None
patent: 63-185940 (1988-08-01), None

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